废水除磷技术的研究与发展

目前 ,人们越来越重视污水除磷技术。本文介绍与评述了化学和生物两种除磷方式及其除磷机理和工艺 ,并着重介绍了生物除磷的现状、发展和研究动向     

藻渣添加对玉米秸秆厌氧发酵特征的影响

厌氧发酵是农业废弃物资源化的有效途径之一.将农业废弃物同其他富含氮元素的有机废物混合发酵能够有效地提高产气效率.以玉米秸秆为例,尝试利用藻渣作为添加剂,提高农业废弃物厌氧发酵的性能.实验主要研究了混合发酵比例对沼气产量、甲烷产量、沼渣沼液特征的影响.当玉米秸秆、藻渣和接种污泥的挥发性固体质量分数为10:2:2时,沼气产率最高可达421.0 mL/g,甲烷产率为218.7 mL/g.沼渣组分分析表明,纤维素和半纤维素降解效率分别为83.7%和68.4%,和对照相比纤维素的降解效率显著提高.结果表明,藻渣的添加能够有效地促进玉米秸秆厌氧发酵产甲烷过程.     

Fenton-混凝法处理焦化废水的试验研究

对Fenton预氧化-混凝法联用技术处理焦化废水进行了研究,探讨了Fenton氧化阶段H2O2投加量、混凝阶段pH值以及混凝剂投加量等因素对焦化废水COD去除率的影响,确定了最佳处理条件.结果表明,Fenton预氧化-混凝法处理焦化废水取得了良好效果,COD去除率达97.5%,为该工艺实际处理焦化废水提供了实验依据.     

层状氢氧化镁铝对偶氮染料酸性黑10B的脱色性能研究

分别用层状氢氧化镁铝(LDH)和焙烧层状氢氧化镁铝(CLDH)作为吸附剂吸附脱除水溶液中偶氮染料酸性黑10B.考察了脱色时间、pH值、吸附剂的投加量、温度、染料初始浓度和焙烧温度等因素对脱色率的影响.结果表明,LDH及CLDH对酸性黑10B染料具有良好的脱除效果,室温下,10g/L LDH和1g/L的CLDH对浓度为100mg/L的染料的脱色率分别达95.93%和99.97%.pH值是影响吸附能力的关键因素,吸附剂对溶液pH值有一定缓冲作用.LDH及CLDH对酸性黑10B吸附结果符合Langmuir吸附等温式.饱和吸附后的LDH及CLDH用高温热解法再生,吸附性能良好,随再生次数增多,脱色率下降.     

Ce-Sn-W-O_x催化剂的配伍优化及脱硝影响因素

采用共混热解法制备系列Ce-Sn-W-Ox复合氧化物,用于NH3选择性催化还原NO。通过正交实验优化CeSn-W-Ox配方,采用环境扫描电镜(ESEM)、X-射线衍射仪(XRD)等表征分析催化剂的微观形貌和固相结构,确立Ce-Sn-WOx最佳配比及结构形貌。结果表明,以粒度为5~8 mm的堇青石瓷片担载分散Ce-Sn-W-Ox,进行NH3-SCR脱除NO,当Ce/Sn/W元素摩尔比为1∶0.8∶0.6时,Ce Sn0.8W0.6Ox/堇青石NH3-SCR脱除NO效果最好。当空速为7 200 h-1,催化剂在252~426℃内脱除NO效率均大于94%。重点考察了反应空速(GHSV)、水蒸气(H2O)、SO2等对Ce Sn0.8W0.6Ox/堇青石NH3-SCR脱除NO活性的影响。研究表明,空速低于10 000 h-1时,催化剂脱硝活性受空速影响小;单独通入5%H2O对催化剂脱硝活性基本没有影响;单独通入429 mg/m3SO2导致催化剂活性略有降低;同时通入429 mg/m3SO2和5%H2O,催化剂脱硝活性下降至85.33%,除去SO2和H2O后,催化剂活性又能明显回升。     

巢湖蓝藻酸提取液提高玉米秸秆的酶解效率

资源化利用是避免富营养化水体打捞得到的蓝藻二次污染的有效方法途径。本研究以巢湖蓝藻为例,利用稀硫酸处理得到酸提取液并将其用于玉米秸秆的酶解过程。以主要成分还原糖和蛋白质的提取量为目标,优化了稀硫酸处理条件(处理时间、温度和硫酸浓度)。结果表明,从巢湖蓝藻提取还原糖的效率随着处理温度和硫酸浓度的升高而升高。在处理温度为125℃,处理时间为2 h,稀硫酸浓度为5%时,提取的还原糖最多为(152.8±12.6)mg/g。稀硫酸处理条件对蛋白质的提取效果影响并不显著。在处理温度为105℃,处理时间为1 h,稀硫酸浓度为5%时,最大提取量为(1.55±0.00)mg/g。提取的藻液中和后可以用于玉米秸秆的酶解过程,同对照相比酶解效率能够提升10%左右。结果表明,藻液中的小分子物质和钙离子是主要的作用组分,推测其和木质素表面官能团结合,从而降低了木质素对纤维素酶的非再生吸附。     

大型垃圾填埋场垃圾稳定化研究

本文对大型垃圾填埋场内不同填埋时间垃圾四个组分 (总糖、有机质、生物可降解物和粗纤维 )含量进行了分析 ,并对各指标随填埋时间的变化趋势进行了讨论。结果表明 :在试验场封场后不久 ,垃圾取样均匀性不能保证 ,各指标随时间变化波动很大 ;封场 71 8d后 ,各指标随时间变化呈现一定的规律性 ,垃圾的生物可降解物含量变化能较好地反映垃圾的降解规律。     

Kinetic modeling of microbially-driven redox chemistry of radionuclides in subsurface environments: coupling transport, microbial metabolism and geochemistry

Microbial reactions play an important role in regulating pore water chemistry as well as secondary mineral distribution in many subsurface systems and, therefore, may directly impact radionuclide migration in those systems. This paper presents a general modeling approach to couple microbial metabolism, redox chemistry, and radionuclide transport in a subsurface environment. To account for the likely achievement of quasi-steady state biomass accumulations in subsurface environments, a modification to the traditional microbial growth kinetic equation is proposed. The conditions for using biogeochemical models with or without an explicit representation of biomass growth are clarified. Based on the general approach proposed in this paper, the couplings of uranium reactions with biogeochemical processes are incorporated into computer code BIORXNTRN Version 2.0. The code is then used to simulate a subsurface contaminant migration scenario, in which a water flow containing both uranium and a complexing organic ligand is recharged into an oxic carbonate aquifer. The model simulation shows that Mn and Fe oxyhydroxides may vary significantly along a flow path. The simulation also shows that uranium(VI) can be reduced and therefore immobilized in the anoxic zone created by microbial degradation.     

浙江省地方环境标准制定思考

地方环境标准是对国家环境标准的补充和完善。为加大污染控制力度,适应新形势下环境管理和执法要求,有效改善和保护环境质量,针对浙江省主要环境问题和现行国家环境标准的不足,结合产业发展方向和环境保护目标,制定浙江省地方环境标准十分必要。主要从浓度控制与排放总量控制相结合、敏感或特殊有毒有害污染物控制、行业污染控制和相关环境质量等方面提出了地方环境标准的制定思路。     

Reactions of compost-derived humic substances with lead, copper, cadmium, and zinc

Thermodynamic stability constants of the formation of complexes from the reactions of humic substances with various metals are usually used as parameters to judge the reactivities of both humic substances and metals. However, in calculating the thermodynamic stability constants, complicated processes for the acquisition of activities of components in reactions are absolutely inevitable. In this study, we investigated the average conditional concentration quotients of the complexes formed from the reaction of metals with humic substances and the relations of these quotients to thermodynamic stability constants. The characterized humic substances including HA (MW>1,000), FA (MW>1,000), and FA (MW<1,000) extracted from a swine compost were prepared to react with Pb, Cu, Cd, and Zn at 25 degrees C and at pH 4.00 and 6.50. Reactions of HA (MW>1,000), FA (MW>1,000), and FA (MW<1,000) with the four metals were carried out at 1:0.1, 1:0.5, 1:1, 1:5, and 1:10 ligand:metal stoichiometry. The concentrations of the free ions of Pb, Cu, Cd, and Zn in the reaction systems of metal-HA suspensions and metal-FA solutions were measured by anodic stripping voltammetry (ASV). The sequence of the average conditional concentration quotients of the formed complexes from the reaction of humic substances with metals was FA(MW<1,000)>FA(MW>1,000)>HA(MW>1,000), showing the relative reactivities of the fractions of swine compost-derived humic substances. The sequence of reacting metals with humic substances was Pb>Cu>Cd>Zn, which is in good agreement with the sequence reported by judging the thermodynamic stability constants. The average conditional concentration quotients of the formed complexes from the reaction of humic substances with metals were thus useful parameters that can be directly related to thermodynamic stability constants and other parameters.